Canonical Allele Identifier: CA2466835771

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154928694T= , CM000685.2:g.154928694T=	GRCh38
NC_000023.10:g.154156969T= , CM000685.1:g.154156969T=	GRCh37
NC_000023.9:g.153810163T=	NCBI36
NG_011403.1:g.99030A=
NG_011403.2:g.99030A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5096A= MANE Select	ENSP00000353393.4:p.Tyr1699=
ENST00000360256.8:c.5096A=	ENSP00000353393.4:p.Tyr1699=
NM_000132.3:c.5096A=	NP_000123.1:p.Tyr1699=
XM_011531126.1:c.4991A=	XP_011529428.1:p.Tyr1664=
NM_000132.4:c.5096A= MANE Select	NP_000123.1:p.Tyr1699=